Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome.

MLA

Colin, Estelle, et al. “Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome.” American Journal of Human Genetics, vol. 95, no. 6, Dec. 2014, pp. 637–48. EBSCOhost, https://doi.org/10.1016/j.ajhg.2014.10.011.

APA

Colin, E., Huynh Cong, E., Mollet, G., Guichet, A., Gribouval, O., Arrondel, C., Boyer, O., Daniel, L., Gubler, M.-C., Ekinci, Z., Tsimaratos, M., Chabrol, B., Boddaert, N., Verloes, A., Chevrollier, A., Gueguen, N., Desquiret-Dumas, V., Ferré, M., Procaccio, V., … Antignac, C. (2014). Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome. American Journal of Human Genetics, 95(6), 637–648. https://doi.org/10.1016/j.ajhg.2014.10.011

Chicago

Colin, Estelle, Evelyne Huynh Cong, Géraldine Mollet, Agnès Guichet, Olivier Gribouval, Christelle Arrondel, Olivia Boyer, et al. 2014. “Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome.” American Journal of Human Genetics 95 (6): 637–48. doi:10.1016/j.ajhg.2014.10.011.